VERIFY STEAM Integrating Indicator— 510(k) K152630
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K152630 for VERIFY STEAM Integrating Indicator, Substantially Equivalent on 2016-05-12. Applicant: STERIS Corporation. Device class: 2.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Product code JOJ
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mentor, OH, US
Recent devices under product code JOJ
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view allRecalls naming K152630
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K152630.
Data sourced from openFDA. This site is unofficial and independent of the FDA.